1. A Novel Splice Variant of Pmel17 Expressed by Human Melanocytes and Melanoma Cells Lacking Some of the Internal Repeats 
Sarah E. Nichols, Dawn C. Harper, Joanne F. Berson, Michael S. Marks 
Journal of Investigative Dermatology 
Volume 121, Issue 4, Pages (October 2003)
DOI: /j x
Copyright © 2003 The Society for Investigative Dermatology, Inc Terms and Conditions

2. Figure 1
Processing of Pmel17 and appearance of band X in untransformed human melanocytes. Primary human foreskin-derived melanocytes were pulse labeled with 35S-methinonine/cysteine for 30 min and then chased for 0, 1, or 4 h in the presence of excess unlabeled methionine and cysteine. Triton X-100 cell lysates (C) or culture supernatants (S) were immunoprecipitated with antibodies to the lumenal (HMB50, lanes 1–5) or cytoplasmic (αPmel-C, lanes 6–10) domains of Pmel17, and immunoprecipitates were analyzed by SDS–PAGE and phosphorimaging. The position of molecular weight markers is indicated in the middle. The positions of the core glycosylated precursor (P1), band X (X), the Golgi-processed P2 form, and the proteolytic products Mα and Mβ are indicated. Arrows, nonreproducible bands that most likely reflect post-lysis degradation products.
Journal of Investigative Dermatology  , DOI: ( /j x)
Copyright © 2003 The Society for Investigative Dermatology, Inc Terms and Conditions

3. Figure 2
Immunoprecipitation/recapture of band X using anti-Pmel17 antibodies. MNT-1 cells were pulse labeled with 35S-methinonine/cysteine for 30 min and then chased for 0 (a) or 2 h (b) with excess unlabeled methionine and cysteine. Triton X-100 cell lysates were immunoprecipitated using the anti-Pmel17 antibodies αPmel-N (lanes 1 and 12), αPmel-C (lanes 2–5 and 13–16), or HMB50 (lanes 6–8 and 17–19), or the anti-Tyrp1 antibody TA99 (lanes 9–11 and 20–22). Material from the first immunoprecipitate was eluted by boiling with SDS and reducing agent, cooled, diluted with Triton X-100 lysis buffer, and subject to a second round of immunoprecipitation using normal rabbit serum (NRS; lanes 5, 8, 11, 16, 19, and 22) or the anti-Pmel17 antibodies αPmel-C (lanes 3, 6, 9, 14, 17, and 20) or αPmel-N (lanes 4, 7, 10, 15, 18, and 21). Material from the first round (lanes 1, 2, 12, and 13) or second round (all other lanes) of immunoprecipitation were fractionated by SDS–PAGE and analyzed by phosphorimaging. The position of molecular weight markers is indicated to the right of each gel, and the migration of the P1, P2, Mα, Mβ, and band X forms of Pmel17 are indicated. Note that (b) was exposed for a longer period of time than (a) in order to emphasize the Mα and Mβ bands.
Journal of Investigative Dermatology  , DOI: ( /j x)
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4. Figure 3
Detection of Pmel17 mRNA with an internal deletion by reverse transcriptase–PCR of mRNA from MNT-1 cells. (a) Schematic diagram of Pmel17 cDNA and position of primers used in this analysis. The noncoding 5′- and 3′-untranslated regions (5′ UT and 3′ UT) are indicated as solid lines, and the coding region is boxed and divided according to the domain structure of the encoded protein. Indicated are the regions encoding the signal peptide; the lumenal domain PKD homology domain, tandem repeat domain, cleavage site separating the Mα and Mβ fragment (CS), and the peptide excised in Pmel17-i; and the transmembrane (TM) and cytoplasmic (Cyt.) domains. The length of our Pmel17-l cDNA is indicated by nucleotide positions 1 and Bottom, the position of the primers, noted in Table I, within the cDNA is indicated, with arrows showing the direction of the primer. Not shown is primer 172, which is the reverse complement of 171. (b) Reverse transcriptase–PCR reactions from MNT-1 mRNA. MNT-1 mRNA was reverse transcribed using primer no. 398 (lanes 1, 4, 10, and 13) or no. 356 (lane 7); a parallel sample was incubated under identical conditions in the absence of reverse transcriptase enzyme (lanes 2, 5, 8, 11, and 14). Reaction products or 100 ng of purified Pmel17-l plasmid (lanes 3, 6, 9, 12, and 15) were subject to 30 cycles of PCR using the indicated forward primers and either no. 356 (lanes 7–9) or no. 398 (all other lanes) as the reverse primer. M, 100 bp markers; arrowhead indicates the 600 bp marker band. Predicted sizes for each of the reaction products for Pmel17-l are 1669, 1265, 524, 444, and 182 bp, respectively.
Journal of Investigative Dermatology  , DOI: ( /j x)
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5. Figure 4
Broad expression of small Pmel17 mRNA in melanocytic cells by reverse transcriptase–PCR. mRNA isolated from the melanoma cell lines MNT-1 (lanes 1–3 and 16–18) or 1011-mel (lanes 4–6), from two different primary foreskin melanocyte cultures (1° FSM-1, lanes 7–9; 1° FSM-2, lanes 10–12), or from nonmelanocytic HeLa cells (lanes 13–15 and 19–21) was reverse transcribed using primer no. 172; parallel reactions were performed identically but with no added reverse transcriptase enzyme (lanes 2, 5, 8, 11, 14, 17, and 20). The products of these reactions or 100 ng of plasmid encoding Pmel17-l (lanes 3, 6, 9, 12, and 15) were subjected to 30 cycles of PCR using primers no. 172 and no. 145 to amplify a region that would best distinguish the short and long forms of Pmel17 (lanes 1–15). The 638 bp reaction product, predicted from the sequence of Pmel17-l, is indicated by a line, and the 510 bp reaction product corresponding to the short form is indicated by an arrow. As a positive control, a 650 bp cDNA fragment for Rab5a was amplified using primers no. 319 and no. 321 from RNA isolated from MNT-1 (lanes 16 and 17) and HeLa cells (lanes 19 and 20); the same reaction was also performed on Pmel17-l plasmid (lanes 18 and 21).
Journal of Investigative Dermatology  , DOI: ( /j x)
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6. Figure 5
Sequence analysis of cDNA corresponding to the small Pmel17 mRNA reveals a deletion of part of the internal repeats. (a) Comparison of the sequence of the small and large Pmel17 mRNA. Shown at top is a schematic of the Pmel17-l cDNA (see Figure 3a for explanation). The indicated region of Pmel17-l and Pmel17-i is expanded below to show the nucleotide and predicted amino acid sequence. The region in bold type is absent from the cDNA isolated for the short form; the nucleotide and predicted amino acid sequence of this region of the short form is indicated at the bottom. Numbers correspond to the nucleotide position of our Pmel17-l cDNA clone and the amino acid positions of the mature protein (with signal peptide removed). (b) Comparison of the direct repeat region in Pmel17-l/PMEL17-i with that predicted from the nucleotide sequence of Pmel17-s. The alternative splice removes 3.5 of the 10 imperfect direct repeats. Numbers correspond to the amino acid positions of the mature protein (with signal peptide removed). (c) Schematic diagram of four Pmel17 mRNA for which the cDNA were isolated from MNT-1 cells. Lumenal, transmembrane (tm) and cytoplasmic (cyto) domains are indicated. Spliced regions are indicated by gray shading.
Journal of Investigative Dermatology  , DOI: ( /j x)
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7. Figure 6
Expression and processing of Pmel17-s in HeLa cells. (a) Immunoprecipitation of three Pmel17 isoforms from metabolically pulse labeled HeLa cells. MNT-1 cells (lanes 2 and 4) or HeLa cells transiently transfected with expression vectors for Pmel17-l (lane 1), Pmel17-i (lane 3), or Pmel17-s (ls form; see Fig. 5clane 5) were labeled for 15 min with 35S-methionine/cysteine. Triton X-100 cell lysates were immunoprecipitated with αPmel-C, fractionated by SDS–PAGE, and analyzed by phosphorimaging. Position of molecular weight markers is indicated to the right, and the positions of the P1 and band X forms of Pmel17 in MNT-1 cells is indicated to the left. (b) Western blot analysis of Pmel17 isoforms expressed in HeLa cells. Whole cell lysates of transiently transfected HeLa cells expressing Pmel17-l, Pmel17-i or Pmel17-s were treated or not with EndoH, fractionated by SDS–PAGE on 12% (upper panel) or 8% (lower panel) polyacrylamide gels, transferred to nitrocellulose using 15% (upper panel) or 2% (lower panel) methanol, and immunoblotted with antibodies to the cytoplasmic domain (Pmel-C, upper panel) or the lumenal domain (Pmel-N, lower panel). Relevant portions of the gels encompassing the P1, Mβ, and Mα isoforms, and of EndoH-digested P1 (P1'), as indicated, are shown; no other specific bands were reproducibly observed. Variation in band intensity is due to different transfection efficiencies, which varied from experiment to experiment.
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8. Figure 7
Immunofluorescence microscopy analyses of the localization of Pmel17-l, Pmel17-i, and Pmel17-s expressed in HeLa cells. Transiently transfected HeLa cells expressing Pmel17-l (a–c), Pmel17-i (d–f), or Pmel17-s (g–i) were fixed and stained with antibodies HMB50 (IgG2a, to Pmel17) and H4A3 (IgG1, to Lamp1) and isotype-specific, fluorochrome-conjugated secondary antibodies (fluorescein isothiocyanate, anti-γ1; Texas Red, anti-γ2a). Cells were analyzed by immunofluorescence microscopy (IFM), and stacks of images in multiple z focal planes were deconvolved using OpenLab software. Shown are individual fields for Lamp1 (a,d,g), Pmel17 (b,e,h), and colorized, merged images (c,f,i). The boxed region in each panel is magnified×2.5 at the bottom right of each panel to emphasize the degree of colocalization. Bar: (a) 10 μm.
Journal of Investigative Dermatology  , DOI: ( /j x)
Copyright © 2003 The Society for Investigative Dermatology, Inc Terms and Conditions